Canonical Allele Identifier: CA603657586
Gene: SLCO1B1 HGNC NCBI

Linked Data

dbSNP Id: rs1179730778
gnomAD v2: 12-21327498-G-T
MyVariant Identifiers: chr12:g.21327498G>T (hg19) chr12:g.21174564G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21174564G>T , CM000674.2:g.21174564G>T GRCh38
NC_000012.11:g.21327498G>T , CM000674.1:g.21327498G>T GRCh37
NC_000012.10:g.21218765G>T NCBI36
NG_011745.1:g.48371G>T , LRG_1022:g.48371G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000256958.3:c.227-13G>T MANE Select ENSP00000256958.2:n.227-13G>T
ENST00000256958.2:c.227-13G>T ENSP00000256958.2:n.227-13G>T
ENST00000543498.5:c.426-2212G>T
NM_006446.4:c.227-13G>T , LRG_1022t1:c.227-13G>T NP_006437.3:n.227-13G>T
NM_006446.5:c.227-13G>T MANE Select NP_006437.3:n.227-13G>T
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